Canonical Allele Identifier: CA474210479
Gene: SLC39A13 HGNC NCBI

Linked Data

dbSNP Id: rs2096021701
MyVariant Identifiers: chr11:g.47436884A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47415333A>G , CM000673.2:g.47415333A>G GRCh38
NC_000011.9:g.47436884A>G , CM000673.1:g.47436884A>G GRCh37
NC_000011.8:g.47393460A>G NCBI36
NG_017073.1:g.11839A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000362021.9:c.1086A>G MANE Select ENSP00000354689.4:p.Val362=
ENST00000354884.8:c.1065A>G ENSP00000346956.4:p.Val355=
ENST00000362021.8:c.1086A>G ENSP00000354689.4:p.Val362=
ENST00000524886.1:n.344A>G
ENST00000524928.1:c.*1416A>G ENSP00000437186.1:n.*1416A>G
ENST00000527829.1:n.446A>G
ENST00000533076.5:c.*83A>G ENSP00000434290.1:n.*83A>G
NM_001128225.2:c.1086A>G NP_001121697.1:p.Val362=
NM_152264.4:c.1065A>G NP_689477.2:p.Val355=
XM_006718381.2:c.1110A>G XP_006718444.1:p.Val370=
XM_006718383.2:c.1002A>G XP_006718446.1:p.Val334=
XM_006718384.2:c.*83A>G XP_006718447.1:n.*83A>G
XM_006718385.2:c.*83A>G XP_006718448.1:n.*83A>G
XM_011520466.1:c.1131A>G XP_011518768.1:p.Val377=
XM_011520467.1:c.1086A>G XP_011518769.1:p.Val362=
XM_011520468.1:c.1086A>G XP_011518770.1:p.Val362=
XM_011520469.1:c.1023A>G XP_011518771.1:p.Val341=
XM_011520470.1:c.978A>G XP_011518772.1:p.Val326=
XR_242832.1:n.1471A>G
XR_428862.2:n.1146A>G
XR_428863.2:n.1142A>G
XR_930928.1:n.1167A>G
NM_001330245.1:c.*83A>G NP_001317174.1:n.*83A>G
NR_134854.1:n.1327A>G
XM_006718381.3:c.1110A>G XP_006718444.1:p.Val370=
XM_006718383.3:c.1002A>G XP_006718446.1:p.Val334=
XM_011520468.3:c.1086A>G XP_011518770.1:p.Val362=
XM_011520470.2:c.978A>G XP_011518772.1:p.Val326=
XM_017018540.2:c.1065A>G XP_016874029.1:p.Val355=
XM_017018541.2:c.957A>G XP_016874030.1:p.Val319=
XM_024448762.1:c.1215A>G XP_024304530.1:p.Val405=
XR_001748027.1:n.1286A>G
XR_001748028.1:n.1268A>G
XR_428862.3:n.1146A>G
XR_428863.3:n.1142A>G
XR_930928.2:n.1167A>G
NM_001128225.3:c.1086A>G MANE Select NP_001121697.2:p.Val362=
NM_001330245.2:c.*83A>G NP_001317174.2:n.*83A>G
NM_152264.5:c.1065A>G NP_689477.3:p.Val355=